A-A-52199
Metric products. Products manufactured to metric dimensions will be considered on an equal basis with those manufactured using inch-pound units, providing they fall within the tolerance specified using conversion tables contained in the latest revision of Federal Standard 376, and all other requirements of this document are met. If a product is manufactured to metric dimensions and those dimensions exceed the tolerances specified in the inch/pound units, a request should be made to the contracting officer to determine if the product is acceptable. The contracting officer has the option of accepting or rejecting the product.
5.5 FDA/NSF International standard compliance. Prior to approval of the first shipment, the contractor shall submit satisfactory evidence to the contracting officer or his authorized representative that the mess trays conform to the applicable requirements of FDA or NSF International Standard No. 2 or No. 36. Acceptable evidence of meeting the requirements of FDA or NSF International Standard No. 2 or No. 36 shall be a listing in the current edition of the NSF International “Listings-Food Service Equipment and Related Products, Components and Materials” and display of the FDA or NSF Product Certification mark on the finished product, or a certified test report from a recognized independent laboratory acceptable to the medical authority of the Government indicating the item complies with the applicable FDA or NSF International requirements. Acceptability of the testing laboratory by the medical authority of the Government will be obtained prior to the award of any contract or procurement document.
5.6 Sampling for examination. The inspection lot shall consist of all trays of the same type and class offered for inspection at one time. A random sample of trays shall be selected from each lot. The sample unit shall be as specified for each examination or test. No more than one tray shall be drawn from any one shipping container.
5.6.1 End item visual examination. The end item sample trays shall be visually examined for the defects listed in table I. The sample unit shall be three (3) trays. Any tray in the end item sample unit containing one or more defects shall be cause for rejection of the lot.
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